Muscular Dystrophy Occurring in Identical Twins
نویسندگان
چکیده
منابع مشابه
Duchenne's muscular dystrophy in monozygotic twins.
Five-year-old twin boys were admitted to our hospital with history of progressive difficulty in walking, climbing stairs and frequent falls. There was delay in the attainment of motor milestones. Both boys had bilateral calf muscle hypertrophy with weakness of proximal muscles of lower and upper limbs. Serum creatinine kinase levels were grossly elevated (>11,000 IU/L) in both boys, and muscle ...
متن کاملNarcolepsy in identical twins.
Narcolepsy has been observed in chronic encephalitis, cerebral arteriosclerosis, brain tumour, and following trauma, but when these cases are excluded there remains a group without demonstrable brain pathology. The existence of this idiopathic group has been a controversial subject. Among the more impressive evidence is that suggesting a hereditary factor in idiopathic narcolepsy. To date this ...
متن کامل[Sarcoidosis in identical twins].
M.R.C.S., F.R.S., and R. B. THOMPSON, M.D., M.R.C.P. .................................................... 605 Fulminating Staphylococcal Pneumonia Associated with Influenza Virus C C. S. DARKE, M.D., M.R.C.P., P. H. WATKINS, B.M., and J. E. M. WHITEHEAD, M.B., DiP.BaCt. ..... ......... 606 Protoveratrine A in Treatment of Hypertension IAN R. GRAY, M.D., M.R.C.P., and NEIL A. J. HAMER, M.B., M.R...
متن کاملIdentical atherosclerotic lesions in identical twins.
In 1997, a 55-year-old man underwent percutaneous coronary angioplasty (PTCA) of a lesion in the middle segment of the left anterior descending coronary artery (LAD) (Figure, A). He subsequently informed his cardiologist that his twin brother had also been treated successfully with PTCA at another hospital for stenosis of the LAD. The cineangiographic film of the twin brother was retrieved (Jac...
متن کاملP164: Adeno-Associated Viral Vectors in Duchenne Muscular Dystrophy
Duchenne muscular dystrophy (BMD) is an inherited X-link disease. The incidence of this muscle-wasting disease is 1:5000 male live births. Mutation in the gene coding for dystrophin is the main cause of BMD. Most cases of this disease succumb to respiratory and cardiac failure in 3rd to 4th decades. The slow progression of BMD and recent achievement of gene therapies make it as an appropriate c...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: BMJ
سال: 1955
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.1.4910.389